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Clutch- Lock 101

FDA UDI

Class I (US FDA UDI)

by Streifeneder ortho.production GmbH

Identity

Trade Name
Clutch- Lock 101 FDA UDI
Generic Name
External lower-limb prosthesis suspensory component, non-powered FDA UDI
Device Name
Clutch-Lock 101 with pin "geared" with lamination dummy, incl. sealing grease FDA UDI
Model / Reference
10S1 FDA UDI
Description
Clutch-Lock 101 with pin "geared" with lamination dummy, incl. sealing grease FDA UDI

Identifiers

Catalog Number
10S1 FDA UDI
Primary DI / UDI-DI
04048817378741 FDA UDI
FDA Product Code
ISY FDA UDI
GMDN Term
External lower-limb prosthesis suspensory component, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: External lower-limb prosthesis suspensory component, non-powered

Clutch- Lock 101 by Streifeneder ortho.production GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External lower-limb prosthesis suspensory component, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Streifeneder ortho.production GmbH

Sources (1)

  • FDA UDI 0024e924-beb2-481f-811a-6a29a6348d04 34 fields · synced Jun 8, 2026